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Angewandte Chemie (International Ed. in English)|January 28, 2025
Enantioselective Borylcupration/Cyclization of Alkene-Tethered Oxime EstersJonathan Bajohr, Shangyu Li, Bijan Mirabi, et al.
Organic Letters|October 16, 2010
C-H bond functionalization in the synthesis of fused 1,2,3-triazolesJane Panteleev, Karolin Geyer, Angelica Aguilar-Aguilar, et al.
Angewandte Chemie (International Ed. in English)|November 21, 2015
An Exclusively trans-Selective Chlorocarbamoylation of Alkynes Enabled by a Palladium/Phosphaadamantane CatalystChristine M Le, Xiao Hou, Theresa Sperger, et al.
Organic Letters|May 24, 2016
A New Multicomponent Multicatalyst Reaction (MC)(2)R: Chemoselective Cycloaddition and Latent Catalyst Activation for the Synthesis of Fully Substituted 1,2,3-TriazolesKosuke Yamamoto, Theodora Bruun, Jung Yun Kim, et al.
Angewandte Chemie (International Ed. in English)|November 8, 2014
Synergistic steric effects in the development of a palladium-catalyzed alkyne carbohalogenation: stereodivergent synthesis of vinyl halidesChristine M Le, Perry J C Menzies, David A Petrone, et al.
Organic Letters|May 23, 2022
Palladium-Catalyzed Three-Component Dearomatization/Sulfonylation CascadeJonathan Bajohr, Matthias D Böhme, Jiacheng Gao, et al.
Angewandte Chemie (International Ed. in English)|December 23, 2021
Dearomative Cyclopropanation of Naphthols via Cyclopropene Ring-OpeningRachel J Baker, Justin Ching, Teh Ren Hou, et al.
The Journal of Organic Chemistry|May 18, 2010
Ligand-controlled selectivity in the desymmetrization of meso cyclopenten-1,4-diols via rhodium(I)-catalyzed addition of arylboronic acidsFrederic Menard, David Perez, Daniela Sustac Roman, et al.
Angewandte Chemie (International Ed. in English)|February 21, 2019
Forming Benzylic Iodides via a Nickel Catalyzed Diastereoselective Dearomative Carboiodination Reaction of IndolesAustin D Marchese, Florian Lind, Áine E Mahon, et al.
Organic Letters|May 25, 2002
Total synthesis of ionomycin using ring-opening strategiesMark Lautens, John T Colucci, Sheldon Hiebert, et al.
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